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Protocol summary
Determining the effectiveness of injectable phenytoin and oral sodium valproate in the acute phase of mania in bipolar patients
Determining the effectiveness of oral phenytoin and oral sodium valproate in the acute phase of mania in bipolar patients
Determining the effectiveness of injectableoral phenytoin and oral sodium valproate in the acute phase of mania in bipolar patients
تعیین اثربخشی فنیتوئین تزریقی و والپروات سدیم خوراکی در فاز حاد مانیا در بیماران دوقطبی
تعیین اثربخشی فنیتوئین خوراکی و والپروات سدیم خوراکی در فاز حاد مانیا در بیماران دوقطبی
تعیین اثربخشی فنیتوئین تزریقیخوراکی و والپروات سدیم خوراکی در فاز حاد مانیا در بیماران دوقطبی
The first group of injectable phenytoin drug will receive an initial dose of 10 mg/kg followed by 100 mg intravenously over 50 minutes every 8 hours and the second group will receive oral sodium valproate at a dose of 20 mg/kg daily for two weeks.
The first group received oral phenytoin with an initial dose of 100 mg/d for one week, and if there is no response to the treatment after one week, the amount of 100 mg will be added to the initial dose on a weekly basis until the dose of 600 mg.
and the second group will receive oral sodium valproate at a dose of 20 mg/kg daily for two weeks.
The first group of injectablereceived oral phenytoin drug will receivewith an initial dose of 10100 mg/kg followed byd for one week, and if there is no response to the treatment after one week, the amount of 100 mg intravenously over 50 minutes every 8 hourswill be added to the initial dose on a weekly basis until the dose of 600 mg. and the second group will receive oral sodium valproate at a dose of 20 mg/kg daily for two weeks.
گروه اول داروی فنیتوئین تزریقی دوز اولیه 10میلی گرم و در ادامه 100 میلی گرم داخل وریدی در طی 50 دقیقه هر 8 ساعت و گروه دوم داروی والپروات سدیم خوراکی را با دوز میلی گرم 20 به صورت روزانه دریافت به مدت دو هفته صورت خواهد گرفت.
گروه اول داروی فنیتوئین خوراکی را با دوز اولیه mg/d 100 به مدت یک هفته دریافت کرده و در صورت عدم پاسخ به درمان پس از یک هفته میزان mg 100 به دوز اولیه به صورت هفتگی تا حداکثر دوز mg 600 اضافه خواهد شد. و گروه دوم داروی والپروات سدیم خوراکی را با دوز میلی گرم 20 به صورت روزانه دریافت به مدت دو هفته صورت خواهد گرفت.
گروه اول داروی فنیتوئین تزریقیخوراکی را با دوز اولیه 10میلی گرمmg/d 100 به مدت یک هفته دریافت کرده و در ادامهصورت عدم پاسخ به درمان پس از یک هفته میزان mg 100 میلی گرم داخل وریدی در طی 50 دقیقه هر 8 ساعتبه دوز اولیه به صورت هفتگی تا حداکثر دوز mg 600 اضافه خواهد شد. و گروه دوم داروی والپروات سدیم خوراکی را با دوز میلی گرم 20 به صورت روزانه دریافت به مدت دو هفته صورت خواهد گرفت.
Intervention groups
#1
Intervention group: Injectable phenytoin drug, the initial dose is 10 mg/kg and then 100 mg/kg intravenously over 50 minutes every 8 hours.
Intervention group:received oral phenytoin with an initial dose of 100 mg/d for one week, and if there is no response to the treatment after one week, the amount of 100 mg will be added to the initial dose on a weekly basis until the dose of 600 mg.
Intervention group: Injectablereceived oral phenytoin drugwith an initial dose of 100 mg/d for one week, and if there is no response to the treatment after one week, the amount of 100 mg will be added to the initial dose is 10on a weekly basis until the dose of 600 mg/kg and then 100 mg/kg intravenously over 50 minutes every 8 hours.
گروه مداخله: داروی فنیتوئین تزریقی دوز اولیه میلی گرم 10 و در ادامه 100 میلی گرم داخل وریدی در طی 50 دقیقه هر 8 ساعت
گروه مداخله: داروی فنیتوئین خوراکی را با دوز اولیه mg/d 100 به مدت یک هفته دریافت کرده و در صورت عدم پاسخ به درمان پس از یک هفته میزان mg 100 به دوز اولیه به صورت هفتگی تا دوز mg 600 اضافه خواهد شد.
گروه مداخله: داروی فنیتوئین تزریقیخوراکی را با دوز اولیه میلی گرم 10mg/d 100 به مدت یک هفته دریافت کرده و در ادامهصورت عدم پاسخ به درمان پس از یک هفته میزان mg 100 میلی گرم داخل وریدی در طی 50 دقیقه هر 8 ساعتبه دوز اولیه به صورت هفتگی تا دوز mg 600 اضافه خواهد شد.
Recruitment centers
#1
Name of recruitment center - English: Ibn Sina Psychiatric Hospital
Name of recruitment center - Persian: بیمارستان روانپزشکی ابن سینا
Full name of responsible person - English: AliManteghi
Full name of responsible person - Persian: علی منطقی
Street address - English: Mashhad, Bu Ali Square, Ibn Sina Psychiatric Hospital
Street address - Persian: مشهد میدان بوعلی بیمارستان روانپزشکی ابن سینا
City - English: MASHHAD
City - Persian: مشهد
Province: Razavi Khorasan
Country: Iran (Islamic Republic of)
Postal code: 99199-91766
Phone: +98 903 926 4520
Fax:
Email: raikaravan@gmail.com
Web page address:
Name of recruitment center - English: Ibn Sina Psychiatric Hospital
Name of recruitment center - Persian: بیمارستان روانپزشکی ابن سینا
Full name of responsible person - English: AliManteghi
Full name of responsible person - Persian: علی منطقی
Street address - English: Ibn Sina Psychiatric Hospital, Bu Ali Square, Mashhad
Street address - Persian: مشهد, میدان بوعلی ,بیمارستان روانپزشکی ابن سینا
City - English: MASHHAD
City - Persian: مشهد
Province: Razavi Khorasan
Country: Iran (Islamic Republic of)
Postal code: 99199-91766
Phone: +98 903 926 4520
Fax:
Email: raikaravan@gmail.com
Web page address:
Name of recruitment center - English: Ibn Sina Psychiatric Hospital Name of recruitment center - Persian: بیمارستان روانپزشکی ابن سینا Full name of responsible person - English: AliManteghi Full name of responsible person - Persian: علی منطقی Street address - English: MashhadIbn Sina Psychiatric Hospital, Bu Ali Square, Ibn Sina Psychiatric HospitalMashhad Street address - Persian: مشهد, میدان بوعلی ,بیمارستان روانپزشکی ابن سینا City - English: MASHHAD City - Persian: مشهد Province: Razavi Khorasan Country: Iran (Islamic Republic of) Postal code: 99199-91766 Phone: +98 903 926 4520 Fax: Email: raikaravan@gmail.com Web page address:
Protocol summary
Study aim
Determining the effectiveness of oral phenytoin and oral sodium valproate in the acute phase of mania in bipolar patients
Design
Clinical trial with control group, with parallel groups, blinded, randomized, phase 2 on 70 patients. The rand function of Excel software was used for randomization
Settings and conduct
Ibn Sina Hospital of Mashhad will be conducted on 70 patients aged 18-40 with bipolar disorder in the acute phase of mania. The disease was diagnosed based on the diagnostic criteria of DSM-5 and the severity of the symptoms will be evaluated on the day of hospitalization and daily during one week of the start of injectable drug treatments.
Participants/Inclusion and exclusion criteria
1. Patients with bipolar disorder in an episode
2. Patients in the age range of 18 to 40
3. Absence of pregnancy and postpartum period
4. Not having medical illness, especially convulsions
Exclusion criteria:
sensitivity to drug treatment
Intervention groups
The first group received oral phenytoin with an initial dose of 100 mg/d for one week, and if there is no response to the treatment after one week, the amount of 100 mg will be added to the initial dose on a weekly basis until the dose of 600 mg.
and the second group will receive oral sodium valproate at a dose of 20 mg/kg daily for two weeks.
Main outcome variables
Patients' symptoms based on daily visits and YMRS, CGI tests
General information
Reason for update
Acronym
IRCT registration information
IRCT registration number:IRCT20101130005280N61
Registration date:2023-03-23, 1402/01/03
Registration timing:registered_while_recruiting
Last update:2023-11-19, 1402/08/28
Update count:2
Registration date
2023-03-23, 1402/01/03
Registrant information
Name
Raheleh Nejati
Name of organization / entity
Mashhad University of Medical Scinces, Ibn-e- Sina Psychiatric Hospital
Country
Iran (Islamic Republic of)
Phone
+98 51 3711 2540
Email address
nejatir2@mums.ac.ir
Recruitment status
Recruitment complete
Funding source
Expected recruitment start date
2023-03-21, 1402/01/01
Expected recruitment end date
2023-07-21, 1402/04/30
Actual recruitment start date
empty
Actual recruitment end date
empty
Trial completion date
empty
Scientific title
A comparative study of the effectiveness of injectable phenytoin and oral sodium valproate in the acute phase of mania in bipolar patients
Public title
Comparative study of the effectiveness of injectable phenytoin
Purpose
Diagnostic
Inclusion/Exclusion criteria
Inclusion criteria:
Patients with bipolar disorder in manic episode based on DSM-5 criteria
Patients should be in the age range of 18 to 40 years
To have the ability to perform and cooperate in psychological tests
Absence of pregnancy and the postpartum period
Not having severe medical illness, especially convulsions
Exclusion criteria:
History of drug sensitivity
Age
From 18 years old to 40 years old
Gender
Both
Phase
1-2
Groups that have been masked
No information
Sample size
Target sample size:
70
Randomization (investigator's opinion)
Randomized
Randomization description
70 patients are randomized in a simple way using a table of random numbers (to use the table of random numbers, first the framework of the statistical community is determined (70 people); respectively, we give them a code or serial number. Codes and numbers It should be equal to that assigned to the members of society; for example, in our research, we give two-digit codes to people, such as 01, 02, 03, ..., 11, 12, ....
To select sample people from the table, we randomly start from a point in the table in the row or column direction. We can choose the point by closing our eyes and placing a finger or the tip of a pen on the table. Moving in the direction of row or column does not differ and this is optional. But according to the type of code digits (one digit, two digit, three digit, etc.), we must choose the same number of digits in the direction of row or column. After this, we control the route numbers. Whether we like it or not, we will come across two types of numbers, one type of which is smaller than the number of the studied community and the other type is larger than the number of the community. We should pay attention to and choose only the smaller numbers. The selected number is actually the code of an individual from the community that is selected as a sample. This work should continue until the number of sample people can be chosen as small as possible. After the sample volume is complete, the sampling work ends.
The numbers will be placed in sealed envelopes, and when the participants enter, an envelope will be assigned to each of them, and they will be placed in one of the 2 intervention groups.
Blinding (investigator's opinion)
Not blinded
Blinding description
Placebo
Not used
Assignment
Parallel
Other design features
Secondary Ids
empty
Ethics committees
1
Ethics committee
Name of ethics committee
Ethics Committee of Mashhad University of Medical Sciences
Street address
Central Building of Mashhad University of Medical Sciences (Ghorshi), Daneshgah 16, Daneshgah Street
City
MASHHAD
Province
Razavi Khorasan
Postal code
9117699199
Approval date
2022-10-23, 1401/08/01
Ethics committee reference number
IR.MUMS.REC.1401.232
Health conditions studied
1
Description of health condition studied
bipolar
ICD-10 code
ICD-10 code description
Primary outcomes
1
Description
Patient symptoms(behavioral stability and depression)
Timepoint
Before the intervention and 48 hours after the intervention
Method of measurement
Based on daily visits and YMRS, CGI tests
Secondary outcomes
empty
Intervention groups
1
Description
Intervention group:received oral phenytoin with an initial dose of 100 mg/d for one week, and if there is no response to the treatment after one week, the amount of 100 mg will be added to the initial dose on a weekly basis until the dose of 600 mg.
Category
Treatment - Other
2
Description
Control group: Valproate sodium medicine will be taken orally at a dose of 20 mg/kg daily for two weeks
Category
Treatment - Other
Recruitment centers
1
Recruitment center
Name of recruitment center
Ibn Sina Psychiatric Hospital
Full name of responsible person
AliManteghi
Street address
Ibn Sina Psychiatric Hospital, Bu Ali Square, Mashhad
City
MASHHAD
Province
Razavi Khorasan
Postal code
99199-91766
Phone
+98 903 926 4520
Email
raikaravan@gmail.com
Sponsors / Funding sources
1
Sponsor
Name of organization / entity
Mashhad University of Medical Sciences
Full name of responsible person
Majid Ghayour
Street address
Central Building of Mashhad University of Medical Sciences (Ghorshi), Daneshgah 16, Daneshgah street
City
MASHHAD
Province
Razavi Khorasan
Postal code
345 -91357
Phone
+98 903 926 4520
Email
raikaravan@gmail.com
Grant name
Grant code / Reference number
Is the source of funding the same sponsor organization/entity?
Yes
Title of funding source
Mashhad University of Medical Sciences
Proportion provided by this source
100
Public or private sector
Public
Domestic or foreign origin
Domestic
Category of foreign source of funding
empty
Country of origin
Type of organization providing the funding
Academic
Person responsible for general inquiries
Contact
Name of organization / entity
Mashhad University of Medical Sciences
Full name of responsible person
Ali Manteghi
Position
Professor
Latest degree
Specialist
Other areas of specialty/work
Psychiatrics
Street address
Ibn Sina Hospital, Bu Ali Square, Mashhad
City
Mashhad
Province
Razavi Khorasan
Postal code
99199-91766
Phone
+98 903 926 4520
Email
raikaravan@gmail.com
Person responsible for scientific inquiries
Contact
Name of organization / entity
Mashhad University of Medical Sciences
Full name of responsible person
AliManteghi
Position
Professor
Latest degree
Specialist
Other areas of specialty/work
Psychiatrics
Street address
Ibn Sina Hospital, Bu Ali Square, Mashhad
City
Mashhad
Province
Razavi Khorasan
Postal code
99199-91766
Phone
+98 903 926 4520
Email
raikaravan@gmail.com
Person responsible for updating data
Contact
Name of organization / entity
Mashhad University of Medical Sciences
Full name of responsible person
Ali Manteghi
Position
Professor
Latest degree
Specialist
Other areas of specialty/work
Psychiatrics
Street address
Ibn Sina Psychiatric Hospital, Bu Ali Square, Mashhad
City
Mashhad
Province
Razavi Khorasan
Postal code
99199-91766
Phone
+98 903 926 4520
Email
raikaravan@gmail.com
Sharing plan
Deidentified Individual Participant Data Set (IPD)
Undecided - It is not yet known if there will be a plan to make this available
Study Protocol
Undecided - It is not yet known if there will be a plan to make this available
Statistical Analysis Plan
Undecided - It is not yet known if there will be a plan to make this available
Informed Consent Form
Undecided - It is not yet known if there will be a plan to make this available
Clinical Study Report
Undecided - It is not yet known if there will be a plan to make this available
Analytic Code
Undecided - It is not yet known if there will be a plan to make this available
Data Dictionary
Undecided - It is not yet known if there will be a plan to make this available